Homozygous calreticulin mutations in patients with myelofibrosis lead to acquired myeloperoxidase deficiency
Autor: | Theocharides, Alexandre P.A., Lundberg, Pontus *, Lakkaraju, Asvin K.K. *, Lysenko, Veronika, Myburgh, Renier, Aguzzi, Adriano, Skoda, Radek C., Manz, Markus G. |
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Zdroj: | In Blood 23 June 2016 127(25):3253-3259 |
Databáze: | ScienceDirect |
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